Crystal structure, magnetic property and DFT analysis for a bis(tetracyanoquinodimethane)zinc(II) complex

• Published in: Polyhedron Vol. 28; no. 9; pp. 1888 - 1892
• Main Authors: Chen, You-Cun, Zhou, Hong-Bo, Liu, Guang-Xiang, Ren, Xiao-Ming, Song, You
• Format: Journal Article
• Language: English
• Published: Elsevier Ltd 22.06.2009
• Subjects: Crystal structure; DFT calculations; Magnetic property; TCNQ radical; Magnetic property; TCNQ radical; DFT calculations; Crystal structure
• ISSN: 0277-5387
• DOI: 10.1016/j.poly.2008.10.020

A bis(tetracyanoquinodimethane)zinc(II) complex shows biradical characteristic and two SOMOs possess small energy gap. A bis(tetracyanoquinodimethane)zinc(II) complex ( 1) was structurally characterized, in which the Zn 2+ ion occupies at an inversion centre and is bonded to two tetracyanoquinodimethane radical anions (TCNQ −), two H 2O and two DMF molecules to form almost perfectly octahedral coordination geometry. The strong H-bonding interactions are observed between H 2O molecules as well as between H 2O molecule and TCNQ − radical anion of the neighboring complex molecules, additionally, there exist π⋯π stack interactions between TCNQ − radical anions. The intermolecular H-bonding and π⋯π stack interactions lead to a supramolecular network sheet forming on the crystallographic ac-plane, and the neighboring supramolecular network sheets further extend into three-dimensional supramolecular structure via weak van der Waals forces. Symmetry-broken approach in the theoretical formwork of DFT for magnetic exchange constants analysis disclosed that the ground state of 1 is singlet state, the excited triplet state is much closed to the nonmagnetic ground state with a small energy gap of 1.25 × 10 −5 eV, and there exist AFM interaction in the TCNQ π-stacks, and these predictions are in agreement with magnetic susceptibility measurements.